Modified release formulation of lacosamide

ABSTRACT

The present invention provides a modified release formulation of lacosamide. The modified release formulation of the present invention comprising lacosamide and modified release polymer provides modified release of lacosamide with minimal C max  to C min  peak to trough variation over a period of at least 12 hrs.

This application is a National Stage Application of PCT/IN2010/000722,filed 3 Nov. 2010, which claims benefit of Serial No. 258/KOL/2010,filed 16 Mar. 2010 in India, and which also claims benefit of Serial No.1309/KOL/2009, filed 3 Nov. 2009 in India and which applications areincorporated herein by reference. To the extent appropriate, a claim ofpriority is made to each of the above disclosed applications.

FIELD OF THE INVENTION

The present invention relates to a modified release formulation ofantiepileptic drug. The formulation of the present invention compriseslacosamide or pharmaceutically acceptable salts, esters, metabolites,prodrugs or enantiomers thereof and modified release polymer.

BACKGROUND OF THE INVENTION

The term epilepsy is derived from a Greek word meaning a condition ofbeing seized or overcome. The term epilepsy designates a group ofcentral nervous system disorders having in common the occurrence ofsudden and transitory episodes of abnormal behavioral symptoms of motorsensory, autonomic or psychic origin. Epilepsies have a definite onsetand ending, and they usually are of short duration.

Epileptic seizures are mainly of two types: partial seizures andgeneralized seizures. Partial seizures can again be of three type; i.e.simple partial, complex partial and partial with secondarily generalizedtonic clonic seizure. Generalized seizures are classified as absenceseizure, myoclonic seizure and tonic-clonic seizure. Anti-epileptic drugare vital in preventing fits for people with epilepsy, thereby greatlyenhancing quality of life.

Based on their mechanism of action, anti-epileptic drugs can beclassified as sodium channel blockers, calcium current inhibitors,gamma-aminobutyric acid (GABA) enhancers, glutamate blockers, carbonicanhydrase inhibitors etc.

Drugs such as acetazolamide, carbamazepine, clobazam, clonazepam,ethosuximide, gabapentin, lamotrigine, levetiracetam, oxcarbazepine,phenobarbital (phenobarbitone), phenyloin, pregabalin, primidone,rufinamide, sodium valproate, tiagabine, topiramate, valproic acid,vigabatrin, zonisamide, valpromide, divalproex sodium, gabapentin,felbamate, fosphenyloin and the like are used for the treatment ofepilepsy.

Anti-epileptic drugs (AEDs) are also promising agents for the preventionof migraine and other head pain. Migraine and epilepsy share severalclinical features and respond to many of the same pharmacologicalagents, suggesting that similar mechanisms may be involved in theirpathophysiology.

The most common side effects associated with epilepsy medicines aredrowsiness, irritability, nausea, rash, and clumsiness. Some drugsproduce changes in emotions, memory or behavior, or affect learning.Modified release formulations of anti-epileptic drugs provides reductionin the above mentioned side effects, increased patient compliance,avoids a typical peak-valley plasma concentration profile and ultimatelyreduction in the precipitation of adverse effects especially of a drugwith a narrow therapeutic index whenever overmedication occurs.

Lacosamide, marketed as Vimpat®, is approved in US for the treatment ofpartial-onset seizure in patient with epilepsy aged 17 years and older.The lacosamide may be used for the treatment or prophylaxis of migraine,fibromyalgia syndrome, osteoarthritis, post herpetic neuralgia andpainful diabetic neuropathy. Chemically lacosamide is(2R)-2-(acetylamino)-3-methoxy-N-(phenylmethyl)propanamide, R-enantiomeris at least 10-fold more active than the S-enantiomer. U.S. Pat. No.5,654,301 discloses aminoacid derivative, lacosamide exhibitinganticonvulsant properties. RE 38,551 discloses the novel enantiomericcompounds one of which is lacosamide.

Vimpat® is approved for oral or intravenous administration. Lacosamidefor oral use has the initial dose of 50 mg twice daily (100 mg per day).It can be increased at weekly intervals by 100 mg/day (two divideddoses) up to the recommended maintenance dose of 200 to 400 mg/day,based on individual patient response and tolerability. The marketedformulation Vimpat® is an immediate release formulation for BIDadministration

The side effect associated with lacosamide is similar to otherepileptics as dizziness, ataxia, vomiting, diplopia, nausea, vertigo andvision blurred.

There exists a need for modified release formulation of lacosamide whichcontrols the release of lacosamide in such a manner that therapeuticallyeffective concentration is maintained in the blood for an extendedperiod of time keeping the drug concentration in the blood substantiallyconstant. The use of modified release formulations of lacosamide wouldimprove patient compliance as it reduces the numbers of dosages to betaken per day.

With the modified release formulation, the therapy may be continuedwithout interrupting the sleep of the patient, which is of specialimportance when treating an epileptic patient to prevent nocturnalseizures, or patients with pain who experience severe pain on awakening,as well as for debilitated patients for whom an uninterrupted sleep isessential.

Thus the modified release formulation of lacosamide would provide amodified release of lacosamide with minimal C_(max) to C_(min) peak totrough variation over a period of at least 12 hrs. It is preferred thatthe modified release formulation of lacosamide is capable of maintaininga substantially constant plasma level of lacosamide for at least 12 hrs.

SUMMARY OF THE INVENTION

In one embodiment, the modified release formulation of lacosamidecomprises lacosamide and modified release polymer.

In other embodiment, the modified release formulation of lacosamidefurther comprises core comprising lacosamide and modified releasecoating.

In another embodiment, the modified release formulation furthercomprises:

-   -   (i) a core comprising non-pareil seed;    -   (ii) coating the non-pareil seed with lacosamide; and    -   (iii) modified release coating.

In further embodiment, the modified release formulation of lacosamidereleases not more than about 25% of lacosamide within 1 hour, from about30% to about 70% of lacosamide within 4 hour and not less than about 75%of lacosamide within 12 hours when tested according to USP type 1dissolution apparatus at 100 rpm and 37° C. temperature in 900 ml of0.1N HCl.

In further embodiment, the modified release formulation comprisinglacosamide and modified release polymer, said modified releaseformulation administered as a single dose provides an invivo plasmaprofile selected from:

-   -   (i) Mean T_(max) of about 5 or more hours, or    -   (ii) Mean C_(max) of less than about 4600 ng/ml, or    -   (iii) Mean AUC₀₋₇₂ of more than about 78500 ng·hr/ml

BRIEF DESCRIPTION OF THE DRAWING

FIG. 01 is a graph depicts the dissolution profile in 0.1N HCl of theformulations as described in Example 03.

FIG. 02 is a graph depicts the mean plasma concentration-time profilesof lacosamide following a single dose of the formulation (QD) in Example3 versus 100 mg of the commercially available immediate release tablet(VIMPAT®).

DETAILED DESCRIPTION OF THE INVENTION

The invention provides a modified release formulation of antiepilepticdrug preferably lacosamide and modified release polymer.

The antiepileptic drug includes sodium channel blockers, calcium currentinhibitors, gamma-aminobutyric acid (GABA) enhancers, glutamateblockers, carbonic anhydrase inhibitors and any other drug which hassimilar action.

The antiepileptic drug can be selected from the group consisting oflacosamide; acetazolamide; carbamazepine; clobazam; clonazepam;ethosuximide; gabapentin; lamotrigine; levetiracetam; oxcarbazepine;phenobarbital (phenobarbitone); phenyloin; pregabalin; primidone;rufinamide; sodium valproate; tiagabine; topiramate; valproic acid;vigabatrin; zonisamide; valpromide; divalproex sodium; gabapentin;felbamate; fosphenyloin; and combination thereof. Other drugs which haveanti epileptic or antimigraine activity are also within the scope of theinvention. The preferred antiepileptic drug is lacosamide.

As used herein the term “lacosamide” refers toN2-acetyl-N-benzyl-D-homoserinamide including its R and S enantiomersand racemic mixtures or pharmaceutically acceptable salts, estres,prodrugs or metabolites. The R enantiomer ofN2-acetyl-N-benzyl-D-homoserinamide is the preferred enantiomer and themarketed immediate release preparation Vimpat® contains the Renantiomer. The modified release formulation preferably contains between10-1000 mg of lacosamide. It has been known that pharmacokinetics oflacosamide is dose proportional at the therapeutic range.

The term “formulation” or “composition” as used herein refers to thedrug in combination with pharmaceutically acceptable excipients. Thisincludes orally administrable formulations as well as formulationsadministrable by other means.

“Modified release formulation” as used herein means a pharmaceuticalformulation which releases the drug substance at a slower rate than froman immediate release formulation.

The term modified release formulation can be used interchangeably withprolonged release formulation, programmed release formulation, timedrelease formulation, extended release formulation, site specific releaseformulation, sustained release formulation, controlled releaseformulation, slow release formulation, delayed release formulation,osmotic dosage form, bioadhesive formulation, orally disintegratingmodified release formulation and other such dosage forms.

The modified release formulation is preferably administered once a day(QD).

“Pharmaceutically acceptable” is meant a carrier comprised of a materialthat is not biologically or otherwise undesirable.

The term “therapeutic effective concentration” is used throughout thespecification to describe concentration of lacosamide which istherapeutically effective in treatment and prophylaxis of diseases wherelacosamide is effective.

The term “relative bioavailability” herein denotes AUC for a specificorally administered composition expressed as a percentage of AUC for anorally administered dosage form of the active ingredient at the samedosage rate.

The terms “AUC₀₋₇₂” herein mean the area under the curve relating bloodplasma concentration to time after administration from 0 to 72 hours, asdetermined using the linear trapezoidal rule, and are expressed in unitsof (ng·h/ml).

The term “AUC_(0-∞)” herein means the area under the curve relatingblood plasma concentration to time from time 0 hours to infinity, and isexpressed in units of (ng·/ml).

The term “AUC_(0-τ)” herein means area under the blood plasmaconcentration to time curve from time zero to time tau over a dosinginterval at steady state, where tau is the length of the dosinginterval, and is expressed in units of (ng·/ml).

The term “C_(max)” herein means the maximum observed blood plasmaconcentration or the maximum blood plasma concentration calculated orestimated from a concentration to time curve, and is expressed in unitsof ng/ml.

The term “C_(min)” herein means the minimum observed blood plasmaconcentration or the maximum blood plasma concentration calculated orestimated from a concentration to time curve, and is expressed in unitsof ng/ml.

The term “C_(avg)” as used herein, means the plasma concentration of thedrug within the dosing interval, and is calculated as AUC/dosinginterval, and is expressed in units of ng/ml.

The term “T_(max)” herein means the time after administration at whichC_(max) occurs, and is expressed in units of hours (h).

The term “single dose” means that the human patient has received asingle dose of the drug formulation and the drug plasma concentrationhas not achieved steady state.

The term “steady state” means that the blood plasma concentration curvefor a given drug does not substantially fluctuate after repeated dosesto dose of the formulation.

The term “Degree of Fluctuation” is expressed as(C_(max)−C_(min))/C_(avg).

The term “bioequivalence” means the absence of a significant differencein the rate and extent to which the active ingredient or active moietyin pharmaceutical equivalents or pharmaceutical alternatives becomesavailable at the site of drug action when administered at the same molardose under similar conditions in an appropriately designed study.

The modified release formulation includes tablets, coated tablets,layered tablets, granules, powders, microparticles, capsules which maybe hard gelatin or soft gelatin, caplets, sachets, pellets, spheroids,mini-tablets, beads, microcapsules and pills.

One embodiment discloses the modified release dosage form of lacosamidecomprising lacosamide and modified release polymer.

Other embodiment discloses the modified release formulation oflacosamide and modified release polymer which provides therapeuticallyeffective concentration of lacosamide for a period of at least 8 hrspreferably 24 hrs or more.

Another embodiment discloses the modified release formulation whichreleases the active ingredient lacosamide—over a period of at least 4hrs, preferably at least 8 hrs and more preferably of at least 12 hrs.

In further embodiment, the modified release formulation comprisinglacosamide and modified release polymer, said modified releaseformulation administered as a single-dose provides an invivo plasmaprofile selected from:

-   -   (i) Mean T_(max) of about 5 or more hours, or    -   (ii) Mean C_(max) of less than about 4600 ng/ml, or    -   (iii) Mean AUC₀₋₇₂ of more than about 78500 ng·hr/ml    -   Lacosamide is administered as a single dose in the dose range of        50 to 800 mg, preferably 100 to 600 mg and more preferably in        the dose of 200 mg.

Further it is contemplated that at given plasma level of lacosamide perspecified dose will be directly proportional to other doses oflacosamide. Such proportional dose and plasma levels are contemplated tobe within the scope of the claimed invention.

The modified release polymer may be selected from hydrophlic polymer,hydrophobic polymer or wax. The hydrophilic polymer may be selected fromthe group consisting of cellulose derivatives such as methyl cellulose,hydroxypropyl methylcellulose (hypromellose), hydroxyethyl cellulose,hydroxypropyl cellulose, hydroxyethyl methylcellulose,carboxymethylcellulose and sodium carboxymethylcellulose; vinylpyrrolidone polymers such as polyvinylpyrrolidone and copolymers ofvinyl pyrrolidone and vinyl acetate; alkylene oxide such as polyethyleneoxide; polysaccharides such as chitosan; gellan; xanthan gum; gums ofplant, animal, mineral or synthetic origin; and alginic acid derivativessuch as alginic acid and its physiologically acceptable salts such assodium, potassium or calcium.

Hydrophobic polymer may be selected from the group consisting of ethylcellulose; cellulose acetate; cellulose acetate butyrate; celluloseacetate phthalate; cellulose acetate trimellitate; polyvinylacetatephthalate; hydroxypropylmethylcellulose phthalate;hydroxypropylmethylcellulose acetate succinate; poly(alkylmethacrylate); poly (vinyl acetate); poly vinyl alcohols; andpolyacrylamide derivatives.

Wax may be selected from the group consisting of glycerolpalmitostearate; beeswax; glycowax; castor wax; carnauba wax; glycerolmonostearate; stearyl alcohol; glycerol behenic acid ester; cetylalcohol; natural and synthetic glycerides; waxes; fatty acids; andhydrogenated vegetable oil.

In one embodiment the modified release polymer used in the modifiedrelease formulation may be bioadhesive.

The bioadhesive polymers may be selected from the group consisting ofproteins (e.g., hydrophilic proteins) such as pectin, zein, modifiedzein, casein, gelatin, gluten, plasma albumin and collagen; chitosan;oligosaccharides; polysaccharides such as cellulose, dextrans, tamarindseed polysaccharide, gellan, carrageenan, xanthan gum, gum arabic,hyaluronic acid, polyhyaluronic acid, alginic acid and sodium alginate;polyamides; polycarbonates; polyalkylenes; polyalkylene glycols;polyalkylene oxides; polyalkylene terephthalates; polyvinyl alcohols;polyvinyl ethers; polyvinyl esters; polyvinyl halides;polyvinylpyrrolidone; polyglycolides; polysiloxanes; polyurethanes;polystyrene; polymers of acrylic and methacrylic esters; polylactides;poly(butyric acid); poly(valeric acid); poly(lactide-co-glycolide);polyanhydrides; polyorthoesters; poly(fumaric acid); poly(maleic acid);and blends or copolymers or mixtures thereof.

Combination of modified release polymers is also included within thescope of the invention.

The amount of modified release polymers may range from about 10-90%.

The modified release formulation may further contain pharmaceuticallyacceptable excipients such as binders; diluents; lubricants;disintegrating agents; glidants; stabilizers; and surface active agents.

The binders may be selected from potato starch; modified starch;gelatin; wheat starch; corn starch; microcrystalline cellulose;celluloses such as hydroxypropyl cellulose, hydroxyethyl cellulose,hydroxypropylmethyl cellulose (Hypromellose), ethyl cellulose and sodiumcarboxy methyl cellulose; natural gums such as acacia, alginic acid andguar gum; liquid glucose; dextrin; povidone; syrup; polyethylene oxide;polyvinyl pyrrolidone; poly vinyl alcohol; poly-N-vinyl amide;polyethylene glycol; gelatin; poly propylene glycol; tragacanth;hydrogenated vegetable oil; castor oil; paraffin; higher aliphaticalcohols; higher alphatic acids; long chain fatty acids; fatty acidesters; and wax-like materials such as fatty alcohols, fatty acidesters, fatty acid glycerides, hydrogenated fats, hydrocarbons, nor-50mal waxes, stearic acid and stearyl alcohol. The amount of binderpresent can vary from about 0.1% to about 25% by weight of the tabletdry weight, preferably about 0.5% to about 10%.

The diluent may be selected from pharmaceutically acceptable inertfillers such as microcrystalline cellulose; lactose; dibasic or tribasiccalcium phosphate; saccharides confectioner's sugar; compressible sugar;dextrates; dextrin; dextrose; fructose; lactitol; mannitol; sucrose;starch xylitol; sorbitol; talc; calcium carbonate; or calcium sulphate.The diluent is preferably used in an amount of about 10 to 90% byweight.

The disintegrating agent may be selected from cross-linked polymers suchas crospovidone; starch or modified starch such as sodium starchglycolate; clays such as bentonite or veegum; celluloses or cellulosederivatives or crosslinked cellulose such as croscarmellose sodium; orresins such as polacrillin potassium.

The lubricant may be selected from Mg, Al or Ca or Zn stearate;polyethylene glycol; glyceryl behenate; glyceryl monosterate; mineraloil; sodium stearyl fumarate; stearic acid; hydrogenated vegetable oil;talc; hydrogenated soybean oil; stearyl alcohol; leucine; polyethyleneglycol; ethylene oxide polymers; or colloidal silica.

The glidant may be selected from magnesium trisilicate; powderedcellulose; starch; talc and tribasic calcium phosphate; calciumsilicate; magnesium silicate; colloidal silicon dioxide; or siliconhydrogel.

The modified release formulation may optionally contain a surface activeagent. The preferred surface active agent may be selected from a groupconsisting of fatty acid; olefin; alkylcarbonyl; silicon elastomer;sulfate ester; petty alcohol sulfate; sulfate pete and oil; sulfonicacid-base; fat sulfonate; alkylaryl sulfonate; ligmin sulfonate;phosphoric acid ester; polyoxyethylene; polyoxyethylene caster oil;polyglycerol; polyol; imidazol; altanolamine; hetamine; sulfobecamine;phosphotide; polyoxyethylene-sorbitan fat acid ester (Tween); andsorbitan ester (Span).

The osmotic agents may be selected from sodium chloride; potassiumchloride; magnesium sulfate; magnesium chloride; sodium sulfate; lithiumsulfate; urea; inositol; sucrose; lactose; glucose; sorbitol; fructose;mannitol; dextrose; magnesium succinate or potassium acid phosphate.

In one of the embodiment the modified release formulation compriseslacosamide and modified release polymer which may optionally coated.

The coating may be modified release coating which may modify the releaseof drug from modified release formulation or coating which does notalter the release of drug from the modified release formulation.

Commercially available, ready-to-coat preparations, sold under variousbrand names such as various grades of Opadry®. Opadry® is a film coatingsystem comprising hypromellose, polyethylene glycol and titanium dioxidewhich does not alter the release of drug from modified releaseformulation may also be used.

Examples of modified release coating include functional coating;moisture barrier coatings; enteric polymeric coatings; sustained releasecoating; and the like.

In one embodiment the modified release formulation further comprisescore comprising lacosamide and modified release coating.

In other embodiment the modified release formulation comprises a corecomprising lacosamide and modified release coating which providestherapeutically effective concentration of lacosamide for a period of atleast 8 hrs preferably 24 hrs or more.

The core may further comprise pharmaceutically acceptable excipients.

In another embodiment, the modified release formulation furthercomprises:

-   -   (i) a core comprising non-pareil seed;    -   (ii) coating the non-pareil seed with lacosamide; and    -   (iii) modified release coating

In another embodiment, the modified release formulation furthercomprises:

-   -   (i) a core comprising non-pareil seed;    -   (ii) coating the non-pareil seed with lacosamide; and    -   (iii) modified release coating        which provides therapeutically effective concentration of        lacosamide for a period of at least 8 hrs preferably 24 hrs or        more.

The non-pareil seed may be selected from sugar spheres, microcrystallinecellulose or other inert material.

The modified release coating comprises of modified release polymer andother pharmaceutically acceptable excipients. The modified releasepolymer includes hydrophilic polymer, hydrophobic polymer or wax asdisclosed above.

The modified release coating composition may comprise of cellulosicpolymer selected form hydroxypropyl cellulose (HPC); hydroxyethylcellulose; hydroxypropyl methylcellulose (hypromellose); methylcellulose; ethyl cellulose; cellulose acetate; cellulose acetatebutyrate; cellulose acetate phthalate; cellulose acetate succinate;cellulose acetate propionate; cellulose acetate trimellitate;hydroxypropylmethyl cellulose phthalate; hydroxypropylmethyl cellulosesuccinate; hydroxypropylmethyl cellulose acetate succinate; celluloseacetate succinate butyrate; cellulose acetate succinate propionate;carboxymethylcellulose sodium, cellulose butyrate; and mixtures thereof;pH-independent acrylates such as Eudragit RS, Eudragit RL and the like;pH-dependent polymers such as poly(methacrylic acid, methylmethacrylate)1:1, poly(methacrylic acid, ethylacrylate) 1:1, poly(methacrylic acid,methylmethacrylate) 1:2, and the like or waxes such as polyethyleneglycol.

The modified release coating may be aqueous, nonaqueous or combinationof the two.

If desired, the permeability of the modified release coating may beadjusted by blending of two or more excipients. The porosity of themodified release coating may be modified by using pore forming agents.The pore forming agents may be selected from crystals of sucrose;mannitol; sorbitol; or salts such as sodium chloride or potassiumchloride.

The modified release coating composition may further include otherpharmacetically acceptable excipients such as plasticizer, solventsystem (i.e., water), a colorant to provide elegance and productdistinction. Color may be added to the solution of the therapeuticallyactive agent instead, or in addition to the overcoat. Suitableingredients for providing color to the formulation include titaniumdioxide and color pigments, such as iron oxide pigments. Theincorporation of pigments, may, however, increase the retard effect ofthe coating. Alternatively, any suitable method of providing color tothe formulations of the present invention may be used.

The plasticizer may be selected from the group consisting of one or moreof polyethylene glycol; triethyl citrate; triacetin; diethyl phthalate;dibutyl stearate; dibutyl sebacate; oleic acid; alcohol; mineral oil;castor oil; lanolin; petrolatum; propylene glycol; and glycerol.

The modified release formulation may be manufactured by various methodsknown in the art such as by dry granulation, wet granulation, meltgranulation, direct compression, double compression, extrusionspheronization, layering and the like. Compaction of the blend intocoprimate may be carried out using a slugging technique or rollercompaction. The milling of the granules may be carried out according toconventional milling methods.

The process of wet granulation includes aqueous or non-aqueous solvents.

The coating operation may be conducted in standard equipment such as afluid bed coater, a wurster coater or a rotary bed coater.

The invention is not to be limited in scope by the specific embodimentsdescribed herein. Indeed, various modifications of the invention inaddition to those described herein will become apparent to those skilledin the art from the foregoing description. Such modifications areintended to fall within the scope of the appended claims.

EXAMPLE 01

Sr. No. Ingredients % w/w 1 Lacosamide 32.26 2 Polyethylene Oxide 24.193 Hypromellose 8.06 4 Mannitol 32.27 5 Colloidal silicon dioxide 1.61 6Magnesium Stearate 1.61 Film Coating: 2-3%Procedure:

-   -   1. Sift all ingredients through suitable sieve    -   2. Blend and mix together Lacosamide, Polyethylene Oxide and        Hypromellose in a suitable blender.    -   3. Add Mannitol to Step 2 and mix till uniform blend is        obtained.    -   4. Mix Step 3 with Colloidal silicon dioxide and lubricate with        Magnesium Stearate for 5 minutes.    -   5. Compress the step 4 into tablet using suitable punch tooling.    -   6. Coat the tablets with coating solution either organic or        aqueous or semiaqueous solution.

EXAMPLE 02

Sr. No. Ingredients % w/w 1 Lacosamide 32.26 2 Microcrystallinecellulose 28.23 3 Polyvinylpyrrolidone 4.03 4 Polyethylene Oxide 24.19 5Hypromellose 8.06 6 Solvent Q.S. 7 Colloidal silicon dioxide 1.61 8Magnesium Stearate 1.61 Film Coating: 2-3%Procedure:

-   -   1. Sift all ingredients through suitable sieve.    -   2. Blend and mix together Lacosamide and Microcrystalline        cellulose in a suitable blender and load in RMG.    -   3. Dissolve and prepare a clear solution of Polyvinylpyrrolidone        in solvent.    -   4. Granulate the Step 2 with the solution from step 3 and dry        the granules in Dryer and mill/size them by passing through        suitable mesh.    -   5. Mix and blend the step 4 with Polyethylene Oxide,        Hypromellose to form a uniform blend.    -   6. Mix Step 5 with Colloidal silicon dioxide and lubricate with        Magnesium Stearate for 5 minutes.    -   7. Compress the step 6 into tablet using suitable punch tooling.    -   8. Coat the tablets with coating solution either organic or        aqueous or semiaqueous solution.

EXAMPLE 03

Sr. No. Ingredients % w/w 1 Lacosamide 19.05 2 Hypromellose 28.57 3Microcrystalline cellulose 23.81 4 Copovidone 23.81 5 Aerosil 2.86 6Magnesium Stearate 1.90 7 Solvent Q.S.Procedure:

-   -   1. Sift Lacosamide, Hypromellose and Microcrystalline cellulose        through 30# sieve.    -   2. Dissolve Copovidone in solvent.    -   3. Granulate step 1 with the solution of step 2.    -   4. Dry the granules at 45° C. and then pass through 20# sieve.    -   5. Sift Microcrystalline cellulose, Crospovidone and Aerosil        through 40# sieve.    -   6. Lubricate step 5 by using Mg-stearate passed through 60#        sieve.    -   7. Compress step 6 by using suitable punch.    -   8. Coat the tablet of Step 7 by using Opadry coating solution        (2-3% wt. Gain)

EXAMPLE 04

Sr. No. Ingredients % w/w 1 Lacosamide 33.33 2 Hydrogenated VegetableOil 8.33 3 Microcrystalline cellulose 34.17 4 Stearic acid 4.17 5Polyethylene glycol 16.67 6 Solvent Q.S. 7 Colloidal silicon dioxide1.67 8 Magnesium Stearate 1.67 Film Coating: 2-3%Procedure:

-   -   1. Sift all ingredients through suitable sieve.    -   2. Add and melt Hydrogenated Vegetable Oil, Polyethylene glycol        and Stearic acid in preheated steam jacketed vessel at 60-70° C.        and to this melted mass, add Lacosamide and stearic acid under        stirring, stop the heating and continue the stirring for 30-45        min until a uniform mass is formed.    -   3. Cool the molten uniform mass to room temperature and mill the        solidify mass in co-mill using suitable sieve.    -   4. Mix and blend the step 3 with Microcrystalline cellulose for        5-10 minutes.    -   5. Mix Step 4 with Colloidal silicon dioxide and lubricate with        Magnesium Stearate for 5 minutes.    -   6. Compress the step 5 into tablet using suitable punch tooling.    -   7. Coat the tablets with coating solution either organic or        aqueous or semiaqueous solution.

EXAMPLE 05

Sr. No. Ingredients % w/w Ist Layer 1 Lacosamide 20.00 2 Hypromellose21.50 3 Microcrystalline cellulose 11.50 4 Copovidone 15.00 5 Aerosil1.00 6 Magnesium Stearate 1.00 7 Solvent Q.S. IInd Layer 1 Polyethyleneoxide 170.59 2 Sodium Chloride 76.47 3 Hypromellose 35.88 4Hydroxypropyl cellulose 9.41 5 Red iron oxide 0.59 6 Magnesium Stearate7.06 7 Solvent Q.S.Procedure:First Layer

-   -   1. Sift Lacosamide, Hypromellose and Microcrystalline cellulose        through 30# sieve.    -   2. Dissolve Copovidone in solvent.    -   3. Granulate step 1 with the solution of step 2.    -   4. Dry the granules at 45° C. and then passed through 20# sieve.    -   5. Sift Crospovidone and Aerosil 200 through 40# sieve.    -   6. Lubricate step 5 by using Magnesium Stearate passed through        60# sieve.        Second Layer    -   1. Sift Polyethylene oxide, Sodium Chloride, Hypromellose,        Hydroxypropyl cellulose and Red iron oxide through 40# sieve.    -   2. Granulate step 1 by using solvent.    -   3. Dry the granules at 45° C. and then passed through 20# sieve.    -   4. Lubricate step 3 by using Magnesium Stearate passed through        60# sieve.        Compression

Compress both layers by using suitable punch

Coating:

Coat the compressed tablet by using Opadry coating solution (2-3% wt.Gain)

EXAMPLE 06

Sr. No. Ingredients % w/w 1 Lacosamide 32.26 2 Microcrystallinecellulose 28.23 3 Polyvinylpyrrolidone 4.03 4 Xanthum Gum 24.19 5Hypromellose 8.06 6 Solvent Q.S. 7 Colloidal silicon dioxide 1.61 8Magnesium Stearate 1.61 Film Coating: 2-3%Procedure:

-   -   1. Sift all ingredients through suitable sieve    -   2. Blend and mix together Lacosamide and Microcrystalline        cellulose in a suitable blender and load in Rapid Mixer        Granulator.    -   3. Dissolve and prepare a clear solution of Polyvinylpyrrolidone        in solvent.    -   4. Granulate the Step 2 with the solution from step 3 and dry        the granules in Dryer and mill/size them by passing through        suitable mesh.    -   5. Mix and blend the step 4 with Xanthum Gum, Hypromellose to        form a uniform blend.    -   6. Mix Step 5 with Colloidal silicon dioxide and lubricate with        Magnesium Stearate for 5 minutes.    -   7. Compress the step 6 into tablet using suitable punch tooling.    -   8. Coat the tablets with coating solution either organic or        aqueous or semiaqueous solution

EXAMPLE 07

Sr. No. Ingredients % w/w 1 Lacosamide 32.26 2 Microcrystallinecellulose 28.23 3 Polyvinylpyrrolidone 4.03 4 Sodium alginate 24.19 5Hypromellose 8.06 6 Solvent Q.S. 7 Colloidal silicon dioxide 1.61 8Magnesium Stearate 1.61 Film Coating: 2-3%Procedure:

-   -   1. Sift all ingredients through suitable sieve.    -   2. Blend and mix together Lacosamide and Microcrystalline        cellulose in a suitable blender and load in Rapid Mixer        Granulator.    -   3. Dissolve and prepare a clear solution of Polyvinylpyrrolidone        in solvent.    -   4. Granulate the Step 2 with the solution from step 3 and dry        the granules in Dryer and mill/size them by passing through        suitable mesh.    -   5. Mix and blend the step 4 with Sodium alginate, Hypromellose        to form a uniform blend.    -   6. Mix the blend of Step 5 with Colloidal silicon dioxide and        lubricate with Magnesium Stearate for 5 minutes.    -   7. Compress the step 6 into tablet using suitable punch tooling.    -   8. Coat the tablets with coating solution either organic or        aqueous or semiaqueous solution.

EXAMPLE 08

Sr. No. Ingredients % w/w Drug loading Spray solution/dispersion 1Lacosamide 13.33 2 Hypromellose 6.66 3 Ethyl cellulose 26.66 4 solventQ.S. 5 Sugar Spheres/Microcrystalline 53.33 Cellulose Spheres Capsulefill Weight 100 Fill the drug loaded pellets in suitable size of capsuleProcedure:

-   -   1. Sift all ingredients through suitable sieve.    -   2. Dissolve and make a clear solution of Lacosamide,        Hypromellose and Ethyl cellulose in solvent under stirring.    -   3. Load Sugar/Microcrystalline Cellulose Spheres in Fluidized        Bed Processor and spray the solution from step 2.    -   4. Fill the capsule with drug-loaded pellets from step 3.

EXAMPLE 09

Sr. No. Ingredients % w/w Drug loading Spray solution/dispersion 1Lacosamide 15.62 2 Hypromellose 15.62 3 Solvent Q.S. Extragranular 4Sugar Spheres/Microcrystalline 62.5 Cellulose Spheres Modified releasecoating with Eudragit Fill the drug loaded pellets in suitable size ofcapsuleProcedure:

-   -   1. Sift all ingredients through suitable sieve.    -   2. Dissolve and make a clear solution of Lacosamide and        Hypromellose in solvent under stirring.    -   3. Load Sugar/Microcrystalline Cellulose Spheres in Fluidized        Bed Processor and spray the solution from step 2.    -   4. Dissolve Eudragit RL, Eudragit RS in solvent and add Dibutyl        Sebacate.    -   5. Fill the above drug loaded pellets in suitable size of        capsule.

EXAMPLE 10

Sr. No. Ingredients % w/w 1 Lacosamide 7.194 2 Microcrystallinecellulose 32.374 4 Hypromellose 32.373 5Polyvinylpyrrolidone/Co-Povidone 3.597 6 Solvent Q.S. 7 Crospovidone14.388 8 Microcrystalline cellulose 7.194 9 Colloidal silicon dioxide1.438 10 Magnesium Stearate 1.438 Modified release coating coating withEudragit: 3-4%Procedure:

-   -   1. Sift all ingredients through suitable sieve    -   2. Blend and mix together Lacosamide, Microcrystalline cellulose        and Hypromellose in a suitable blender and load in Rapid Mixer        Granulator.    -   3. Dissolve and prepare a clear solution of Polyvinylpyrrolidone        in solvent.    -   4. Granulate the Step 2 with the solution from step 3 and dry        the granules in Dryer and mill/size them by passing through        suitable mesh.    -   5. Mix and blend the step 4 with Co-Povidone, Hypromellose and        Microcrystalline cellulose to form a uniform blend.    -   6. Mix Step 5 with Colloidal silicon dioxide and lubricate with        Magnesium Stearate for 5 minutes.    -   7. Compress the step 6 into tablet using suitable punch tooling.    -   8. Coat the tablets with above modified release coating solution        prepared by dissolving Amino-methacrylate co-polymer type A and        type B, Dibutyl sebacate/Triethyl citrate/Polyethylene glycol in        an above mentioned solvent.

EXAMPLE 11

Sr. No. Ingredients % w/w 1 Lacosamide 7.19 2 Microcrystalline cellulose32.37 3 Hypromellose 32.37 4 Polyvinylpyrrolidone/Co-Povidone 3.597 5Solvent Q.S. 6 Crospovidone 14.38 7 Microcrystalline cellulose 7.194 8Colloidal silicon dioxide 1.438 9 Magnesium Stearate 1.438 Modifiedrelease coating with Eudragit: 7-8%Procedure:

-   -   1. Sift all ingredients through suitable sieve.    -   2. Blend and mix together Lacosamide and Microcrystalline        cellulose in a suitable blender and load in Rapid Mixer        Granulator.    -   3. Dissolve and prepare a clear solution of Polyvinylpyrrolidone        in solvent.    -   4. Granulate the Step 2 with the solution from step 3 and dry        the granules in Dryer and mill/size them by passing through        suitable mesh.    -   5. Mix and blend the step 4 with Co-Povidone, Hypromellose and        Microcrystalline cellulose to form a uniform blend.    -   6. Mix Step 5 with Colloidal silicon dioxide and lubricate with        Magnesium Stearate for 5 minutes.    -   7. Compress the step 6 into tablet using suitable punch tooling.    -   8. Coat the tablets with modified release coating dispersion        prepared by Methacrylic acid co-polymer dispersion, Triethyl        citrate, Talc and water.

EXAMPLE 12

Dissolution Study for Lacosamide Tablets of Example 03

The dissolution profile of the 200 mg lacosamide tablets of Example 03was carried out in type 1 dissolution apparatus, basket, at 100 rpm, ata temperature of about 37° C., in 900 ml of 0.1N HCl and may release notmore than about 25% of lacosamide within 1 hour, from about 30% to about70% of lacosamide is released within 4 hour and not less than about 75%of lacosamide is released within 12 hours. The results of the in vitrodissolution profile are set forth in Table: 01 and illustrated in FIG.01

TABLE 01 Dissolution profile of lacosamide 200 mg modified releasetablets of Example 03 Time (Hrs) Avg. % Drug Release 0 0 1 15 2 21.9 438.5 6 46.7 8 59.2 10 66.5 12 72.9 14 81.1 16 88.3

EXAMPLE 13

Clinical Study for Lacosamide Tablets of Example 03:

A single dose study was conducted in healthy human volunteers to assessbioavailability of lacosamide formulated as the 200 mg QD modifiedrelease tablets of Examples 3 by comparison with a reference treatmentwith Vimpat® 100 mg tablet BID (each tablet containing lacosamide 100mg—one tablet each 12 hourly) manufactured for UCB, GA, administeredunder fed conditions in healthy, adult, male, human subjects in arandomized cross over study and to evaluate safety and tolerability oflacosamide when its absorption profile is altered as in these modifiedrelease tablets.

The study design was open label, balanced, randomized, three treatment,three sequence, three-period, single dose crossover bioequivalence studyin 12 healthy, adult, male, human subjects under fed conditions.

The pharmacokinetic parameters AUC₀₋₇₂, AUC_(0-∞), C_(max), and T_(max)were estimated during the study.

Geometric mean plasma lacosamide concentrations over the 72-hourassessment period are shown in FIG. 02. The pharmacokinetic parameterscalculated from mean plasma lacosamide concentration-time profile aregiven in Table: 02.

TABLE 02 Pharmacokinetic parameters (mean ± standard deviation) Test(Lacosamide 200 mg modified release tablet Reference (Vimpat ® T/RParameter (QD)—Example 3) 100 mg tablet(BID) (%) AUC₀₋₇₂ 100606.90 ±21882.72 102700.93 ± 25661.12 97.96 (ng · h/ml) AUC_(0-∞) 109263.99 ±24438.17 113722.90 ± 27763.30 96.08 (ng · h/ml) C_(max) (ng/ml) 3799.61± 733.15 3631.46 ± 380.59 104.63 T_(max) (h) 12.00 4.50 —

The relative bioavailability of the Example 3 formulation to Vimpat® was97.96% in terms of AUC₀₋₇₂ ratio.

The mean plasma lacosamide concentration profile shown in FIG. 02clearly shows the tablets of Example 3 effectively modified the releaseof lacosamide relative to the immediate release tablet (Vimpat®)

The invention claimed is:
 1. A once daily modified release formulationcomprising lacosamide as only active ingredient and at least two releasemodifying polymers, wherein the modified release formulation releases a.not more than about 25% of lacosamide within 1 hour, b. from about 30%to about 70% of lacosamide within 4 hours, and c. not less than about75% of lacosamide within 12 hours when measured in USP type Idissolution apparatus, in 900 mL of 0.1 N HCl at 100 rpm, whereinlacosamide is present in an amount of about 13% to about 33% relative tothe total weight of the formulation, and the at least two releasemodifying polymers are present in an amount of about 12% to about 52%relative to the total weight of the formulation and is selected from thegroup consisting of hydroxypropyl methylcellulose, polyethylene oxide,polyvinylpyrrolidone, ethyl cellulose, copolymers of vinyl pyrrolidone,an alginic acid derivative, hydrogenated vegetable oil and a combinationthereof, and wherein the modified release formulation is in tablet orcapsule form.
 2. The once daily modified release formulation of claim 1,wherein the at least two release modifying polymers are hydroxypropylmethylcellulose is present in an amount of about 28% relative to thetotal weight of the formulation and the copolymers of vinyl pyrrolidoneis present in an amount of about 24% relative to the total weight of theformulation, and wherein the copolymers of vinyl pyrrolidone iscopovidone.
 3. The oral daily modified release formulation of claim 1,wherein the at least two release modifying polymers are hydroxypropylmethylcellulose is present in an amount of about 7% relative to thetotal weight of the formulation and ethyl cellulose is present in anamount of about 27% relative to the total weight of the formulation. 4.The oral daily modified release formulation of claim 1, wherein the atleast two release modifying polymers are hydroxypropyl methylcelluloseis present in an amount of about 8% relative to the total weight of theformulation and polyethylene oxide is present in an amount of about 24%relative to the total weight of the formulation.
 5. The once dailymodified release formulation of claim 1, wherein a single dose comprisesabout 100 mg to 600 mg of lacosamide.
 6. The once daily modified releaseformulation of claim 1, wherein the modified release formulationcomprises a core comprising lacosamide and a modified release coating.7. The once daily modified release formulation of claim 1, wherein themodified release formulation comprises: (i) a core comprising non-pareilseed; (ii) a coating disposed on the non-pareil seed with lacosamide;and (iii) a modified release coating.
 8. The once daily modified releaseformulation of claim 1, wherein the modified release formulationcomprises 100 mg to 600 mg of lacosamide; which when administered to ahuman subject provides an in-vivo plasma profile selected from: (i) MeanT_(max) of about 5 or more hours, or (ii) Mean C_(max) of less thanabout 4600 ng/ml, or (iii) Mean AUC₀₋₇₂ of more than about 78500ng·hr/ml.
 9. The once daily modified release formulation of claim 1,wherein the at least two release modifying polymers are hydroxypropylmethylcellulose is present in an amount of about 8% relative to thetotal weight of the formulation, polyethylene oxide is present in anamount of about 24% relative to the total weight of the formulation, andpolyvinylpyrrolidone is present in an amount of about 4% relative to thetotal weight of the formulation of polyvinylpyrrolidone and the oraldaily modified release formulation further comprising microcrystallinecellulose is present in an amount of about 28% relative to the totalweight of the formulation.
 10. The once daily modified releaseformulation of claim 1, wherein the at least two release modifyingpolymers are hydroxypropyl methylcellulose is present in an amount ofabout 8% relative to the total weight of the formulation,polyvinylpyrrolidone is present in an amount of about 4% relative to thetotal weight of the formulation and an alginic acid derivative ispresent in an amount of about 24% relative to the total weight of theformulation, wherein the alginic acid derivative is sodium alginate. 11.The once daily modified release formulation of claim 1, furthercomprising a diluent, and the diluent is present in an amount of about23% to about 34% relative to the total weight of the formulation. 12.The once daily modified release formulation of claim 11, wherein thediluent is microcrystalline cellulose.
 13. The once daily modifiedrelease formulation of claim 12, wherein the microcrystalline celluloseis present in an amount of about 23% to about 28% relative to the totalweight of the formulation.
 14. The once daily modified releaseformulation of claim 1, further comprising a lubricant.
 15. The oncedaily modified release formulation of claim 14, wherein the lubricantcomprises magnesium stearate.
 16. The once daily modified releaseformulation of claim 1, further comprising a glidant.
 17. The once dailymodified release formulation of claim 16, wherein the glidant comprisescolloidal silicon dioxide.
 18. The once daily modified releaseformulation of claim 1, wherein the copolymers of vinyl pyrrolidonepolymer is copovidone.
 19. The oral daily modified release formulationof claim 1, wherein the at least two release modifying polymers arepolyethylene glycol is present in an amount of about 17% relative to thetotal weight of the formulation, hydrogenated vegetable oil is presentin an amount of about 8% relative to the total weight of theformulation, stearic acid is present in an amount of about 4% relativeto the total weight of the formulation, and microcrystalline celluloseis present in the amount of about 34% relative to the total weight ofthe formulation.
 20. The oral daily modified release formulation ofclaim 1, wherein the at least two release modifying polymers arehydroxypropyl methylcellulose is present in an amount of about 28%relative to the total weight of the formulation and the copolymers ofvinyl pyrrolidone polymer is present in an amount of about 24% relativeto the total weight of the formulation, wherein the copolymers of vinylpyrrolidone polymer is copovidone.
 21. The oral daily modified releaseformulation of claim 1, wherein the at least two release modifyingpolymers are hydroxypropyl methylcellulose is present in an amount ofabout 28% relative to the total weight of the formulation andmicrocrystalline cellulose is present in an amount of about 24% relativeto the total weight of the formulation, and the copolymers of vinylpyrrolidone polymer is present in an amount of about 24% relative to thetotal weight of the formulation, wherein the copolymers of vinylpyrrolidone polymer is copovidone.
 22. The once daily modified releaseformulation of claim 1, further comprising about mannitol.
 23. The oncedaily modified release formulation of claim 22, wherein the mannitol ispresent in an amount of about 32% relative to the total weight of theformulation.
 24. The once daily modified release formulation of claim18, wherein the copovidone is present in an amount of about 24% relativeto the total weight of the formulation.
 25. The once daily modifiedrelease formulation of claim 3, further comprising sugarspheres/microcrystalline cellulose spheres in an amount of about 53%relative to the total weight of the formulation.